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rs868014

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs868014(C;C)
Make rs868014(C;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position11789390
GeneC1orf167, MTHFR
is asnp
is mentioned by
dbSNPrs868014
dbSNP (classic)rs868014
ClinGenrs868014
ebirs868014
HLIrs868014
Exacrs868014
Gnomadrs868014
Varsomers868014
LitVarrs868014
Maprs868014
PheGenIrs868014
Biobankrs868014
1000 genomesrs868014
hgdprs868014
ensemblrs868014
geneviewrs868014
scholarrs868014
googlers868014
pharmgkbrs868014
gwascentralrs868014
openSNPrs868014
23andMers868014
23andMe allrs868014
SNPshotrs868014
SNPdbers868014
MSV3drs868014
GWAS Ctlgrs868014
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 28171870] Methylene Tetrahydrofolate Reductase (MTHFR) rs868014 Polymorphism Regulated by miR-1203 Associates with Risk and Short Term Outcome of Ischemic Stroke.


ClinVar
Risk rs868014(C;C)
Alt rs868014(C;C)
Reference Rs868014(T;T)
Significance Non-pathogenic
Disease Neural tube defects
Variation info
Gene MTHFR C1orf167
CLNDBN Neural tube defects, folate-sensitive
Reversed 1
HGVS NC_000001.10:g.11849447A>G
CLNSRC
CLNACC RCV000277799.1,